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JOIMAX Versicon Spine-Pump - Indonesia BPOM Medical Device Registration

JOIMAX Versicon Spine-Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801411845. The device is manufactured by JOIMAX GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDTEK.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
JOIMAX Versicon Spine-Pump
Analysis ID: AKL 20801411845

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

JOIMAX GMBH

Country of Origin

Germany

Authorized Representative

MEDTEK

AR Address

Delta Building, Blok A-11, C-1 dan C-2, Jl. Suryopronoto No. 1-9

Registration Date

Oct 09, 2023

Expiry Date

Dec 31, 2025

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Radiation Electromedics

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